Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126262621 | 12626262 | 1 | I | 201601 | 20160701 | 20160805 | 20160805 | EXP | US-ASTRAZENECA-2016SE83895 | ASTRAZENECA | 17.00 | MON | M | Y | 0.00000 | 20160805 | CN | MX | MX |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126262621 | 12626262 | 1 | PS | SYNAGIS | PALIVIZUMAB | 1 | Intramuscular | U | 0 | INJECTION | |||||||||
| 126262621 | 12626262 | 2 | SS | SYNAGIS | PALIVIZUMAB | 1 | Intramuscular | U | 0 | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126262621 | 12626262 | 1 | Premature baby |
| 126262621 | 12626262 | 2 | Premature baby |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126262621 | 12626262 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126262621 | 12626262 | Pneumonia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126262621 | 12626262 | 1 | 20151209 | 201601 | 0 | |
| 126262621 | 12626262 | 2 | 20160210 | 0 |